C₂₉H₃₈N₈O₂S₂

Base Information

Chemical Name:C₂₉H₃₈N₈O₂S₂
CAS No.:815579-76-1
Molecular Formula:C₂₉H₃₈N₈O₂S₂
Molecular Weight:594.805
Hs Code.:

C<sub>29</sub>H<sub>38</sub>N<sub>8</sub>O<sub>2</sub>S<sub>2</sub>

Synonyms:C₂₉H₃₈N₈O₂S₂

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₉H₃₈N₈O₂S₂

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Technology Process of C₂₉H₃₈N₈O₂S₂

There total 11 articles about C₂₉H₃₈N₈O₂S₂ which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 22.0%

: 59944-65-9
4-methyl-[1,2,3]thiadiazole-5-carbonyl chloride

: 681291-95-2
C₂₁H₃₄N₄

: 815579-76-1
C₂₉H₃₈N₈O₂S₂

Guidance literature:: 4-methyl-[1,2,3]thiadiazole-5-carbonyl chloride; C₂₁H₃₄N₄; With triethylamine; In dichloromethane; at 0 - 20 ℃; for 1.25h;

With sodium hydroxide; In dichloromethane; water; at 20 ℃; for 0.25h;

Reference yield:

: 193201-63-7
(±)-7-(phenylmethyl)-1,4-dioxa-8-azaspiro[4.5]decane

: 815579-76-1
C₂₉H₃₈N₈O₂S₂

Guidance literature:: Multi-step reaction with 8 steps

1.1: toluene / 20 °C

2.1: ethanol; water / 20 h / 60 °C

3.1: pyrographite / 2 h / 40 °C

3.2: 20 - 50 °C

4.1: hydrogen / palladium 10% on activated carbon

5.1: thiophene; hydrogen / palladium 10% on activated carbon / methanol / 50 °C

6.1: hydrogen / palladium 10% on activated carbon / methanol

7.1: potassium hydroxide / isopropyl alcohol / 18 h / Heating / reflux

8.1: triethylamine / dichloromethane / 1.25 h / 0 - 20 °C

8.2: 0.25 h / 20 °C

With thiophene; potassium hydroxide; hydrogen; pyrographite; triethylamine; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; water; isopropyl alcohol; toluene;

Reference yield:

: 681291-91-8
(+)-(2R-trans)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-[4-(phenylmethyl)-1-piperazinyl]piperidine

: 815579-76-1
C₂₉H₃₈N₈O₂S₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen / palladium 10% on activated carbon

2.1: thiophene; hydrogen / palladium 10% on activated carbon / methanol / 50 °C

3.1: hydrogen / palladium 10% on activated carbon / methanol

4.1: potassium hydroxide / isopropyl alcohol / 18 h / Heating / reflux

5.1: triethylamine / dichloromethane / 1.25 h / 0 - 20 °C

5.2: 0.25 h / 20 °C

With thiophene; potassium hydroxide; hydrogen; triethylamine; palladium 10% on activated carbon; In methanol; dichloromethane; isopropyl alcohol;